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The importance of copy number variation in congenital heart disease
Congenital heart disease (CHD) is the most common class of major malformations in humans. The historical association with large chromosomal abnormalities foreshadowed the role of submicroscopic rare copy number variations (CNVs) as important genetic causes of CHD. Recent studies have provided robust...
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| Gepubliceerd in: | NPJ Genom Med |
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| Hoofdauteurs: | , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Nature Publishing Group
2016
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5505728/ https://ncbi.nlm.nih.gov/pubmed/28706735 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/npjgenmed.2016.31 |
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